WordNet

a horses manner of moving
a persons manner of walking
inability to coordinate voluntary muscle movements; unsteady movements and staggering gait (同)ataxy, dyssynergia, motor_ataxia

PrepTutorEJDIC

《所有・所属》…『の』,…のものである,…に属する・《材料・要素》…『でできた』,から成る・《部分》…『の』[『中の』] ・《数量・単位・種類を表す名詞に付いて》…の・《原因・動機》…『で』,のために(because of) ・《主格関係》…『の』,による,によって・《目的格関係》…『を』,の・《同格関係》…『という』・《関係・関連》…『についての』[『の』],の点で・《抽象名詞などと共に》…の[性質をもつ] ・《『It is』+『形』+『of』+『名』+『to』 doの形で,ofの後の名詞を意味上の主語として》・《分離》…『から』・《起原・出所》…『から』[『の』](out of) ・《『名』+『of』+『a』(『an』)+『名』の形で》…のような・《『名』+『of』+『mine』(『yours, his』など独立所有格)の形で》…の…・《時》(1)《副詞句を作って》…に《形容詞句を作って》…の・《時刻》《米》…前(to,《米》before)
歩きぶり,足どり
OLD French古[代]フランス語

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Kim JS.SourceStroke Center and Department of Neurology, University of Ulsan, Asan Medical Center, Seoul, South Korea.
Frontiers of neurology and neuroscience.Front Neurol Neurosci.2014;33:82-102. doi: 10.1159/000351905. Epub 2013 Oct 11.
Transient ischemic attack (TIA) is a cerebrovascular disease with temporary (<24 h) neurological symptoms. The symptoms of TIA patients are largely similar to those of ischemic stroke patients and include unilateral limb weakness, speech disturbances, sensory symptoms, visual disturbances, and ga
PMID 24157558

Prasad M, Ong MT, Setty G, Whitehouse WP.SourceDepartment of Paediatrics, Dewsbury District Hospital, , Dewsbury, UK.
Archives of disease in childhood. Education and practice edition.Arch Dis Child Educ Pract Ed.2013 Dec;98(6):217-23. doi: 10.1136/archdischild-2013-304653. Epub 2013 Aug 23.
Acute ataxia is a relatively common presentation to the paediatric acute services or child neurologist. Although the cause of ataxia is most often benign, it is important during initial assessment to recognise or exclude serious causes including brain tumour and central nervous system infections. It
PMID 23975413

Reply to comment "why do patients with cerebellar ataxia not use environmental cues for reducing unpredictability of sudden gait stopping?" on "sudden stopping in patients with cerebellar ataxia".

Serrao M, Conte C, Casali C, Ranavolo A, Mari S, Di Fabio R, Perrotta A, Coppola G, Padua L, Monamì S, Sandrini G, Pierelli F.SourceDepartment of Medical and Surgical Sciences and Biotechnologies, University of Rome Sapienza, Latina, Italy, mariano.serrao@uniroma1.it.
Cerebellum (London, England).Cerebellum.2013 Dec;12(6):958-9. doi: 10.1007/s12311-013-0501-z.
PMID 23771603

Clinically Mild form of Joubert Syndrome-related Disorder in a 7-year-old Female:A case report

George Imataka,Yoshiyuki Watabe,Osamu Arisaka
Dokkyo journal of
… Joubert syndrome-related disorders (JSRD) is a very rare syndrome observed with agenesis of the vermis,episodic hyperpnea, abnormal eye movements, and cerebellar ataxia and mental retardation. … There have been many reports on the image-based diagnosis using MRI/CT, but not many clinical reports on the intelligence of subjects with JSRD. … We herein report a clinically mild form of JSRD in a 7-year-old female. …
NAID 110009443674

坂田英明,遠藤まゆみ,加我君孝
Equilibrium Research 71(4), 253-263, 2012
… Abstract Childhood vertigo and disequilibrium are overlooked in many cases because children rarely complain of them. …
NAID 130002127645

Italiano Domenico,Tarantino Patrizia,Valeria De Marco Elvira,Salvatore Calabrò Rocco,Bramanti Placido,Quattrone Aldo,Annesi Grazia
Internal Medicine 51(20), 2953-2955, 2012
… Spinocerebellar ataxia type 7 (SCA7) is a neurodegenerative disorder characterized by degeneration of the cerebellum, brainstem and retina. … We herein describe a family from southern Italy whose proband was a 49-year-old man presenting with ataxia with progressive gait disturbances, clumsiness and visual impairment. … Our study confirms the marked anticipation previously observed in SCA7 and extends the small number of patients studied thus far. …
NAID 130002062092